Genetics, Vol. 166, 1571-1579, March 2004, Copyright © 2004

Stochastic Tunnels in Evolutionary Dynamics

Yoh Iwasaa, Franziska Michorb, and Martin A. Nowakb
a Department of Biology, Kyushu University, Fukuoka 812-8581, Japan
b Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts 02138

Corresponding author: Yoh Iwasa, Kyushu University, Fukuoka 812-8581, Japan., yiwasscb{at}mbox.nc.kyushu-u.ac.jp (E-mail)

Communicating editor: J. B. WALSH

We study a situation that arises in the somatic evolution of cancer. Consider a finite population of replicating cells and a sequence of mutations: type 0 can mutate to type 1, which can mutate to type 2. There is no back mutation. We start with a homogeneous population of type 0. Mutants of type 1 emerge and either become extinct or reach fixation. In both cases, they can generate type 2, which also can become extinct or reach fixation. If mutation rates are small compared to the inverse of the population size, then the stochastic dynamics can be described by transitions between homogeneous populations. A "stochastic tunnel" arises, when the population moves from all 0 to all 2 without ever being all 1. We calculate the exact rate of stochastic tunneling for the case when type 1 is as fit as type 0 or less fit. Type 2 has the highest fitness. We discuss implications for the elimination of tumor suppressor genes and the activation of genetic instability. Although our theory is developed for cancer genetics, stochastic tunnels are general phenomena that could arise in many circumstances.





This article has been cited by other articles:


Home page
GeneticsHome page
R. Durrett and D. Schmidt
Waiting for Two Mutations: With Applications to Regulatory Sequence Evolution and the Limits of Darwinian Evolution
Genetics, November 1, 2008; 180(3): 1501 - 1509.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
Y. Zhao and R. J. Epstein
Programmed Genetic Instability: A Tumor-Permissive Mechanism for Maintaining the Evolvability of Higher Species through Methylation-Dependent Mutation of DNA Repair Genes in the Male Germ Line
Mol. Biol. Evol., August 1, 2008; 25(8): 1737 - 1749.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. M. Desai, D. Weissman, and M. W. Feldman
Evolution Can Favor Antagonistic Epistasis
Genetics, October 1, 2007; 177(2): 1001 - 1010.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
K. Jain and J. Krug
Deterministic and Stochastic Regimes of Asexual Evolution on Rugged Fitness Landscapes
Genetics, March 1, 2007; 175(3): 1275 - 1288.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. H. Bielas, K. R. Loeb, B. P. Rubin, L. D. True, and L. A. Loeb
From the Cover: Human cancers express a mutator phenotype
PNAS, November 28, 2006; 103(48): 18238 - 18242.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
F. Michor, Y. Iwasa, and M. A. Nowak
The age incidence of chronic myeloid leukemia can be explained by a one-mutation model
PNAS, October 3, 2006; 103(40): 14931 - 14934.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
R. A. Beckman and L. A. Loeb
Negative Clonal Selection in Tumor Evolution
Genetics, December 1, 2005; 171(4): 2123 - 2131.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
D. M. Weinreich
The Rank Ordering of Genotypic Fitness Values Predicts Genetic Constraint on Natural Selection on Landscapes Lacking Sign Epistasis
Genetics, November 1, 2005; 171(3): 1397 - 1405.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. Masel
Evolutionary Capacitance May Be Favored by Natural Selection
Genetics, July 1, 2005; 170(3): 1359 - 1371.
[Abstract] [Full Text] [PDF]